valsartan

Generic: valsartan

Labeler: archis pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name valsartan
Generic Name valsartan
Labeler archis pharma llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

valsartan 40 mg/1

Manufacturer
Archis Pharma LLC

Identifiers & Regulatory

Product NDC 72819-181
Product ID 72819-181_0037a1a4-d769-2567-e063-6394a90a721c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205347
Listing Expiration 2026-12-31
Marketing Start 2022-09-01

Pharmacologic Class

Established (EPC)
angiotensin 2 receptor blocker [epc]
Mechanism of Action
angiotensin 2 receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72819181
Hyphenated Format 72819-181

Supplemental Identifiers

RxCUI
349199 349200 349201 349483
UPC
0372819183091
UNII
80M03YXJ7I
NUI
N0000000070 N0000175561

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name valsartan (source: ndc)
Generic Name valsartan (source: ndc)
Application Number ANDA205347 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET, COATED in 1 BOTTLE, PLASTIC (72819-181-03)
source: ndc

Packages (1)

72819-181-03 30 TABLET, COATED in 1 BOTTLE, PLASTIC (72819-181-03)

Ingredients (1)

valsartan (40 mg/1)

Linked Drug Pages (1)

Valsartan ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0037a1a4-d769-2567-e063-6394a90a721c", "openfda": {"nui": ["N0000000070", "N0000175561"], "upc": ["0372819183091"], "unii": ["80M03YXJ7I"], "rxcui": ["349199", "349200", "349201", "349483"], "spl_set_id": ["00b235b2-a909-4628-b37c-bb02bc5bf7c6"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Archis Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (72819-181-03)", "package_ndc": "72819-181-03", "marketing_start_date": "20220901"}], "brand_name": "Valsartan", "product_id": "72819-181_0037a1a4-d769-2567-e063-6394a90a721c", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72819-181", "generic_name": "valsartan", "labeler_name": "Archis Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valsartan", "active_ingredients": [{"name": "VALSARTAN", "strength": "40 mg/1"}], "application_number": "ANDA205347", "marketing_category": "ANDA", "marketing_start_date": "20220901", "listing_expiration_date": "20261231"}